Imaging the preterm infant's brain

Infants born very prematurely (gestational age <32 weeks) are at risk of brain injury and neurodevelopmental problems. Imaging the preterm infant__s brain during the neonatal period, using cranial ultrasonography (cUS) and magnetic resonance imaging (MRI), is important. Our aim was to study and describe brain findings in very preterm infants using modern, high-quality imaging techniques. Part I reviews brain maturation and injury, and imaging thereof, in very preterm infants. Part II discusses our experience on neonatal cUS (Chapters 2-3) and MRI (Chapter 4), and addresses indications, technical aspects, protocols and safety. Part III gives an overview of findings (incidence and evolution) on frequent, sequential neonatal cUS and term-equivalent MRI (Chapter 5), and their relation with perinatal factors (Chapter 6). Part IV focuses on imaging of white matter (Chapters 7-9), describing both normal maturational phenomena and pathological changes and assessing the accuracy of cUS and MRI for these changes. Part V focuses on imaging of deep grey matter (Chapters 10-12), describing both normal maturational phenomena and pathological changes on cUS and assessing their relation with clinical and MRI findings. Part VI reviews the main findings and conclusions of this thesis, and discusses future perspectives and proposals for further research (Chapter 13).PhD: ZonMw, the Netherlands Organization for Health Research and Development (grant number 920-03-388), and The Doctor Catharina van Tussenbroek Foundation Thesis: J.E. Jurriaanse Stichting, Prelum Uitgevers, Nutricia Nederland BV, Foundation ImagoUBL - phd migration 201

Cranial Ultrasonography in Neonates: Role and Limitations

Epidemiology in Pediatrics and Child Healt

Brain ultrasound findings in neonates treated with intrauterine transfusion for fetal anaemia

Epidemiology in Pediatrics and Child Healt

Diffuse Hyperechogenicity of Basal Ganglia and Thalami in Preterm Neonates: A Physiologic Finding?

Purpose: To elucidate whether echogenicity (EG) of the basal ganglia and thalami (BGT) represents a physiologic phenomenon in preterm neonates (<32 weeks gestation). Materials and Methods: The study was approved by the medical ethics committee, and informed consent was obtained from the parents. Sequential neonatal cranial ultrasonographic (US) images obtained in 130 preterm neonates were evaluated for EG of the BGT. In 110 of the 130 neonates, MR imaging was performed around or within the first months after term-equivalent age to assess myelination and changes in BGT signal. Cranial US studies obtained in 83 low-risk near-term neonates were used for comparison. Results: Diffuse homogeneous bilateral EG of the BGT was seen in 120 (92%) of 130 preterm neonates and in seven (8%) of 83 low-risk neonates (P < .001). In preterm neonates, EG of the BGT faded with age and was no longer seen 1 month after delivery. This finding was associated with frontal echodensity, which is a normal prematurity-related cranial US phenomenon that occurs in the white matter (P < .001). No association with changes on MR images was found. Conclusion: In preterm neonates, diffuse homogeneous EG of the BGT is a frequent and normal prematurity-related finding.Neuro Imaging Researc

Lenticulostriate vasculopathy in very preterm infants

Objective: To assess for lenticulostriate vasculopathy (LSV) on cranial ultrasound (cUS) scans of very preterm infants: incidence and aetiology, evolution during neonatal period, association with clinical parameters, and MRI equivalent. Design: Prospective study. Setting: Tertiary neonatal referral centre. Patients: Very preterm infants (7 postnatal days). Perinatal clinical parameters were collected for all infants and compared between groups. Results: In 22/111 (20%) infants LSV was detected: early-onset in 5 and late-onset in 17. LSV mostly presented some weeks after birth and persisted for several months. There were no associations between LSV and other changes on cUS or deer) grey matter changes on MRI, Infants with late-onset LSV were younger and smaller at birth than infants with early-onset LSV. Postmenstrual age at first detection was comparable for both LSV groups. There were no associations between LSV and perinatal clinical parameters, but infants with LSV had less episodes of hypotension than infants without LSV. Conclusions: LSV is a frequent finding on cUS in very preterm infants, but does not show on MRI. The postmenstrual age, rather than gestational and postnatal age, seems important in LSV development. LSV is not associated with clinical parameters, When encountered in otherwise healthy preterm infants, LSV is probably a benign temporary phenomenon.Neuro Imaging Researc

Lenticulostriate vasculopathy in very preterm infants

OBJECTIVE: To assess for lenticulostriate vasculopathy (LSV) on cranial ultrasound (cUS) scans of very preterm infants: incidence and aetiology, evolution during neonatal period, association with clinical parameters, and MRI equivalent. DESIGN: Prospective study. SETTING: Tertiary neonatal referral centre. PATIENTS: Very preterm infants (<32 weeks) underwent sequential cUS throughout the neonatal period and MRI around term age. cUS were evaluated for LSV and other changes, and MRI for changes in signal and myelination in deep grey matter. LSV was divided into early-onset (7 postnatal days). Perinatal clinical parameters were collected for all infants and compared between groups. RESULTS: In 22/111 (20%) infants LSV was detected: early-onset in 5 and late-onset in 17. LSV mostly presented some weeks after birth and persisted for several months. There were no associations between LSV and other changes on cUS or deep grey matter changes on MRI. Infants with late-onset LSV were younger and smaller at birth than infants with early-onset LSV. Postmenstrual age at first detection was comparable for both LSV groups. There were no associations between LSV and perinatal clinical parameters, but infants with LSV had less episodes of hypotension than infants without LSV. CONCLUSIONS: LSV is a frequent finding on cUS in very preterm infants, but does not show on MRI. The postmenstrual age, rather than gestational and postnatal age, seems important in LSV development. LSV is not associated with clinical parameters. When encountered in otherwise healthy preterm infants, LSV is probably a benign temporary phenomenon.Neuro Imaging Researc

Lenticulostriate vasculopathy in very preterm infants

Objective: To assess for lenticulostriate vasculopathy (LSV) on cranial ultrasound (cUS) scans of very preterm infants: incidence and aetiology, evolution during neonatal period, association with clinical parameters, and MRI equivalent. Design: Prospective study. Setting: Tertiary neonatal referral centre. Patients: Very preterm infants (7 postnatal days). Perinatal clinical parameters were collected for all infants and compared between groups. Results: In 22/111 (20%) infants LSV was detected: early-onset in 5 and late-onset in 17. LSV mostly presented some weeks after birth and persisted for several months. There were no associations between LSV and other changes on cUS or deer) grey matter changes on MRI, Infants with late-onset LSV were younger and smaller at birth than infants with early-onset LSV. Postmenstrual age at first detection was comparable for both LSV groups. There were no associations between LSV and perinatal clinical parameters, but infants with LSV had less episodes of hypotension than infants without LSV. Conclusions: LSV is a frequent finding on cUS in very preterm infants, but does not show on MRI. The postmenstrual age, rather than gestational and postnatal age, seems important in LSV development. LSV is not associated with clinical parameters, When encountered in otherwise healthy preterm infants, LSV is probably a benign temporary phenomenon

Small Cerebellar Hemorrhage in Preterm Infants: Perinatal and Postnatal Factors and Outcome

Epidemiology in Pediatrics and Child Healt

Clinical Implications of MR Imaging Findings in the White Matter in Very Preterm Infants: A 2-year Follow-up Study

Epidemiology in Pediatrics and Child Healt